digeorge syndrome Gene Set

Dataset	OMIM Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A T cell deficiency disease that is the result of a large deletion of chromosome 22 which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production. (Human Disease Ontology, DOID_11198)
External Link	http://www.omim.org/entry/188400
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Genes

1 genes associated with the digeorge syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol	Name
TBX1	T-box 1